Accuracy of prognostic serological biomarkers in predicting liver fibrosis severity in people with metabolic dysfunction-associated steatotic liver disease : a meta-analysis of over 40,000 participants

Detalhes bibliográficos
Autor(a) principal: López Tórrez, Sergio
Data de Publicação: 2024
Outros Autores: Ayala, Camila Ospina, Ruggiro, Paula Bayer, Costa, Caroline Abud Drumond, Wagner, Mario Bernardes, Padoin, Alexandre Vontobel, Mattiello, Rita
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/272884
Resumo: Introduction: A prognostic model to predict liver severity in people with metabolic dysfunction-associated steatotic liver disease (MASLD) is very important, but the accuracy of the most commonly used tools is not yet well established. Objective: The meta-analysis aimed to assess the accuracy of different prognostic serological biomarkers in predicting liver fibrosis severity in people with MASLD. Methods: Adults ≥18 years of age with MASLD were included, with the following: liver biopsy and aspartate aminotransferase-to-platelet ratio (APRI), fibrosis index-4 (FIB-4), non-alcoholic fatty liver disease fibrosis score (NFS), body mass index, aspartate aminotransferase/alanine aminotransferase ratio, diabetes score (BARD score), FibroMeter, FibroTest, enhanced liver fibrosis (ELF), Forns score, and Hepascore. Meta-analyses were performed using a random effects model based on the DerSimonian and Laird methods. The study’s risk of bias was assessed using the Quality Assessment of Diagnostic Accuracy Studies-2. Results: In total, 138 articles were included, of which 86 studies with 46,514 participants met the criteria for the meta-analysis. The results for the summary area under the receiver operating characteristic (sAUROC) curve, according to the prognostic models, were as follows: APRI: advanced fibrosis (AF): 0.78, any fibrosis (AnF): 0.76, significant fibrosis (SF): 0.76, cirrhosis: 0.72; FIB-4: cirrhosis: 0.83, AF: 0.81, AnF: 0.77, SF: 0.75; NFS: SF: 0.81, AF: 0.81, AnF: 0.71, cirrhosis: 0.69; BARD score: SF: 0.77, AF: 0.73; FibroMeter: SF: 0.88, AF: 0.84; FibroTest: SF: 0.86, AF: 0.78; and ELF: AF: 0.87. Conclusion: The results of this meta-analysis suggest that, when comparing the scores of serological biomarkers with liver biopsies, the following models showed better diagnostic accuracy in predicting liver fibrosis severity in people with MASLD: FIB-4 for any fibrosis, FibroMeter for significant fibrosis, ELF for advanced fibrosis, and FIB-4 for cirrhosis.
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spelling López Tórrez, SergioAyala, Camila OspinaRuggiro, Paula BayerCosta, Caroline Abud DrumondWagner, Mario BernardesPadoin, Alexandre VontobelMattiello, Rita2024-03-05T04:36:46Z20242296-861Xhttp://hdl.handle.net/10183/272884001196889Introduction: A prognostic model to predict liver severity in people with metabolic dysfunction-associated steatotic liver disease (MASLD) is very important, but the accuracy of the most commonly used tools is not yet well established. Objective: The meta-analysis aimed to assess the accuracy of different prognostic serological biomarkers in predicting liver fibrosis severity in people with MASLD. Methods: Adults ≥18 years of age with MASLD were included, with the following: liver biopsy and aspartate aminotransferase-to-platelet ratio (APRI), fibrosis index-4 (FIB-4), non-alcoholic fatty liver disease fibrosis score (NFS), body mass index, aspartate aminotransferase/alanine aminotransferase ratio, diabetes score (BARD score), FibroMeter, FibroTest, enhanced liver fibrosis (ELF), Forns score, and Hepascore. Meta-analyses were performed using a random effects model based on the DerSimonian and Laird methods. The study’s risk of bias was assessed using the Quality Assessment of Diagnostic Accuracy Studies-2. Results: In total, 138 articles were included, of which 86 studies with 46,514 participants met the criteria for the meta-analysis. The results for the summary area under the receiver operating characteristic (sAUROC) curve, according to the prognostic models, were as follows: APRI: advanced fibrosis (AF): 0.78, any fibrosis (AnF): 0.76, significant fibrosis (SF): 0.76, cirrhosis: 0.72; FIB-4: cirrhosis: 0.83, AF: 0.81, AnF: 0.77, SF: 0.75; NFS: SF: 0.81, AF: 0.81, AnF: 0.71, cirrhosis: 0.69; BARD score: SF: 0.77, AF: 0.73; FibroMeter: SF: 0.88, AF: 0.84; FibroTest: SF: 0.86, AF: 0.78; and ELF: AF: 0.87. Conclusion: The results of this meta-analysis suggest that, when comparing the scores of serological biomarkers with liver biopsies, the following models showed better diagnostic accuracy in predicting liver fibrosis severity in people with MASLD: FIB-4 for any fibrosis, FibroMeter for significant fibrosis, ELF for advanced fibrosis, and FIB-4 for cirrhosis.application/pdfengFrontiers in nutrition. Lausanne, Switzerland. Vol. 11 (2024), 1284509, 25 p.PrognósticoFígadoBiópsiaFigado gordurosoDoenças metabólicasTestes de função hepáticaMetanálisePrognosisLiver biopsyMetabolic dysfunction-associated steatotic liver diseaseNon-invasive testsMeta-analysisAccuracy of prognostic serological biomarkers in predicting liver fibrosis severity in people with metabolic dysfunction-associated steatotic liver disease : a meta-analysis of over 40,000 participantsEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001196889.pdf.txt001196889.pdf.txtExtracted Texttext/plain116128http://www.lume.ufrgs.br/bitstream/10183/272884/3/001196889.pdf.txta9467da4b4a73511e822b7148f08e511MD53001196889-02.pdf.txt001196889-02.pdf.txtExtracted Texttext/plain107409http://www.lume.ufrgs.br/bitstream/10183/272884/4/001196889-02.pdf.txtdb562e1444bfa0315ff0a31df066a02dMD54ORIGINAL001196889.pdfTexto completo (inglês)application/pdf3288408http://www.lume.ufrgs.br/bitstream/10183/272884/1/001196889.pdf9dcbba40792e5c84f0eaf567e2e495abMD51001196889-02.pdfMaterial suplementarapplication/pdf8227776http://www.lume.ufrgs.br/bitstream/10183/272884/2/001196889-02.pdf29ede986a1338187340fd28ecd53f6e6MD5210183/2728842024-03-06 04:55:24.326461oai:www.lume.ufrgs.br:10183/272884Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2024-03-06T07:55:24Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Accuracy of prognostic serological biomarkers in predicting liver fibrosis severity in people with metabolic dysfunction-associated steatotic liver disease : a meta-analysis of over 40,000 participants
title Accuracy of prognostic serological biomarkers in predicting liver fibrosis severity in people with metabolic dysfunction-associated steatotic liver disease : a meta-analysis of over 40,000 participants
spellingShingle Accuracy of prognostic serological biomarkers in predicting liver fibrosis severity in people with metabolic dysfunction-associated steatotic liver disease : a meta-analysis of over 40,000 participants
López Tórrez, Sergio
Prognóstico
Fígado
Biópsia
Figado gorduroso
Doenças metabólicas
Testes de função hepática
Metanálise
Prognosis
Liver biopsy
Metabolic dysfunction-associated steatotic liver disease
Non-invasive tests
Meta-analysis
title_short Accuracy of prognostic serological biomarkers in predicting liver fibrosis severity in people with metabolic dysfunction-associated steatotic liver disease : a meta-analysis of over 40,000 participants
title_full Accuracy of prognostic serological biomarkers in predicting liver fibrosis severity in people with metabolic dysfunction-associated steatotic liver disease : a meta-analysis of over 40,000 participants
title_fullStr Accuracy of prognostic serological biomarkers in predicting liver fibrosis severity in people with metabolic dysfunction-associated steatotic liver disease : a meta-analysis of over 40,000 participants
title_full_unstemmed Accuracy of prognostic serological biomarkers in predicting liver fibrosis severity in people with metabolic dysfunction-associated steatotic liver disease : a meta-analysis of over 40,000 participants
title_sort Accuracy of prognostic serological biomarkers in predicting liver fibrosis severity in people with metabolic dysfunction-associated steatotic liver disease : a meta-analysis of over 40,000 participants
author López Tórrez, Sergio
author_facet López Tórrez, Sergio
Ayala, Camila Ospina
Ruggiro, Paula Bayer
Costa, Caroline Abud Drumond
Wagner, Mario Bernardes
Padoin, Alexandre Vontobel
Mattiello, Rita
author_role author
author2 Ayala, Camila Ospina
Ruggiro, Paula Bayer
Costa, Caroline Abud Drumond
Wagner, Mario Bernardes
Padoin, Alexandre Vontobel
Mattiello, Rita
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv López Tórrez, Sergio
Ayala, Camila Ospina
Ruggiro, Paula Bayer
Costa, Caroline Abud Drumond
Wagner, Mario Bernardes
Padoin, Alexandre Vontobel
Mattiello, Rita
dc.subject.por.fl_str_mv Prognóstico
Fígado
Biópsia
Figado gorduroso
Doenças metabólicas
Testes de função hepática
Metanálise
topic Prognóstico
Fígado
Biópsia
Figado gorduroso
Doenças metabólicas
Testes de função hepática
Metanálise
Prognosis
Liver biopsy
Metabolic dysfunction-associated steatotic liver disease
Non-invasive tests
Meta-analysis
dc.subject.eng.fl_str_mv Prognosis
Liver biopsy
Metabolic dysfunction-associated steatotic liver disease
Non-invasive tests
Meta-analysis
description Introduction: A prognostic model to predict liver severity in people with metabolic dysfunction-associated steatotic liver disease (MASLD) is very important, but the accuracy of the most commonly used tools is not yet well established. Objective: The meta-analysis aimed to assess the accuracy of different prognostic serological biomarkers in predicting liver fibrosis severity in people with MASLD. Methods: Adults ≥18 years of age with MASLD were included, with the following: liver biopsy and aspartate aminotransferase-to-platelet ratio (APRI), fibrosis index-4 (FIB-4), non-alcoholic fatty liver disease fibrosis score (NFS), body mass index, aspartate aminotransferase/alanine aminotransferase ratio, diabetes score (BARD score), FibroMeter, FibroTest, enhanced liver fibrosis (ELF), Forns score, and Hepascore. Meta-analyses were performed using a random effects model based on the DerSimonian and Laird methods. The study’s risk of bias was assessed using the Quality Assessment of Diagnostic Accuracy Studies-2. Results: In total, 138 articles were included, of which 86 studies with 46,514 participants met the criteria for the meta-analysis. The results for the summary area under the receiver operating characteristic (sAUROC) curve, according to the prognostic models, were as follows: APRI: advanced fibrosis (AF): 0.78, any fibrosis (AnF): 0.76, significant fibrosis (SF): 0.76, cirrhosis: 0.72; FIB-4: cirrhosis: 0.83, AF: 0.81, AnF: 0.77, SF: 0.75; NFS: SF: 0.81, AF: 0.81, AnF: 0.71, cirrhosis: 0.69; BARD score: SF: 0.77, AF: 0.73; FibroMeter: SF: 0.88, AF: 0.84; FibroTest: SF: 0.86, AF: 0.78; and ELF: AF: 0.87. Conclusion: The results of this meta-analysis suggest that, when comparing the scores of serological biomarkers with liver biopsies, the following models showed better diagnostic accuracy in predicting liver fibrosis severity in people with MASLD: FIB-4 for any fibrosis, FibroMeter for significant fibrosis, ELF for advanced fibrosis, and FIB-4 for cirrhosis.
publishDate 2024
dc.date.accessioned.fl_str_mv 2024-03-05T04:36:46Z
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dc.relation.ispartof.pt_BR.fl_str_mv Frontiers in nutrition. Lausanne, Switzerland. Vol. 11 (2024), 1284509, 25 p.
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